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Optogenetic protein clustering and signaling activation in mammalian cells

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TLDR
An optogenetic method based on Arabidopsis thaliana cryptochrome 2 for rapid and reversible protein oligomerization in response to blue light is reported, suggesting a previously unknown mode of activation for this Rho GTPase.
Abstract
We report an optogenetic method based on Arabidopsis thaliana cryptochrome 2 for rapid and reversible protein oligomerization in response to blue light. We demonstrated its utility by photoactivating the β-catenin pathway, achieving a transcriptional response higher than that obtained with the natural ligand Wnt3a. We also demonstrated the modularity of this approach by photoactivating RhoA with high spatiotemporal resolution, thereby suggesting a previously unknown mode of activation for this Rho GTPase.

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Optical control of mammalian endogenous transcription and epigenetic states

TL;DR: The development of light-inducible transcriptional effectors (LITEs), an optogenetic two-hybrid system integrating the customizable TALE DNA-binding domain with the light-sensitive cryptochrome 2 protein and its interacting partner CIB1 from Arabidopsis thaliana, establishes a novel mode of optogenetics control of endogenous cellular processes and enables direct testing of the causal roles of genetic and epigenetic regulation in normal biological processes and disease states.
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Spatiotemporal Control of Intracellular Phase Transitions Using Light-Activated optoDroplets

TL;DR: An optogenetic platform that uses light to activate IDR-mediated phase transitions in living cells to elucidate not only physiological phase transitions but also their link to pathological aggregates is introduced.
Journal ArticleDOI

Photoactivatable CRISPR-Cas9 for optogenetic genome editing

TL;DR: An engineered photoactivatable Cas9 that enables optogenetic control of CRISPR-Cas9 genome editing in human cells is described and activation of paCas9 in spatial patterns determined by the sites of irradiation is demonstrated.
Journal ArticleDOI

Engineering an improved light-induced dimer (iLID) for controlling the localization and activity of signaling proteins

TL;DR: The use of computational protein design, phage display, and high-throughput binding assays are described to create an improved light inducible dimer (iLID) that changes its affinity for SspB by over 50-fold with light stimulation.
References
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Journal ArticleDOI

The small GTP-binding protein rho regulates the assembly of focal adhesions and actin stress fibers in response to growth factors.

Anne J. Ridley, +1 more
- 07 Aug 1992 - 
TL;DR: Rho, a ras-related GTP-binding protein, rapidly stimulated stress fiber and focal adhesion formation when microinjected into serum-starved Swiss 3T3 cells, implying that rho is essential specifically for the coordinated assembly of focal adhesions and stress fibers induced by growth factors.
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Polyvalent Interactions in Biological Systems: Implications for Design and Use of Multivalent Ligands and Inhibitors.

TL;DR: Polyvalent interactions can be collectively much stronger than corresponding monovalent interactions, and they can provide the basis for mechanisms of both agonizing and antagonizing biological interactions that are fundamentally different from those available inmonovalent systems.
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Rho GTPases: Biochemistry and Biology

TL;DR: This review presents the best characterized of these biochemical pathways that control some of the most fundamental processes of cell biology common to all eukaryotes, including morphogenesis, polarity, movement, and cell division.
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Cell adhesion: integrating cytoskeletal dynamics and cellular tension

TL;DR: Adhesion formation and disassembly drive the migration cycle by activating Rho GTPases, which in turn regulate actin polymerization and myosin II activity, and therefore adhesion dynamics.
Journal ArticleDOI

Survival and differentiation of adult neuronal progenitor cells transplanted to the adult brain.

TL;DR: It is indicated that FGF-2 responsive progenitors can be isolated from the adult hippocampus and that these cells retain the capacity to generate mature neurons when grafted into the adult rat brain.
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